Is UP & UP FDA approved?

UP & UP holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.

What drugs does UP & UP make?

3 products are listed under UP & UP in the openFDA NDC Directory, most often as tablet, chewable; capsule, delayed release. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

UP & UP

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 0
Active NDC listings: 3
Live patents: 0
Countries: 0

Catalogue

Drug listings by form and route

3 active NDC listings: 3 human otc drug. By marketing category: ANDA 3.

Dosage form	NDCs
tablet, chewable	2
capsule, delayed release	1

Route	NDCs
oral	3

Labeller name on the listing	NDCs
up & up	3

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
DYE-FREE CHILDRENS LORATADINE	LORATADINE	tablet, chewable, oral	11673-111ANDA
Dye-Free Childrens Loratadine	LORATADINE	tablet, chewable, oral	11673-115ANDA
Omeprazole	Omeprazole Magnesium	capsule, delayed release, oral	11673-948ANDA

Compare

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Enquiry

Common questions

Is UP & UP FDA approved?: UP & UP holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does UP & UP make?: 3 products are listed under UP & UP in the openFDA NDC Directory, most often as tablet, chewable; capsule, delayed release. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.